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$165k - $200k
...Sr Manager / Associate Director, GMP Quality Assurance Join to apply for the Sr Manager / Associate Director, GMP Quality Assurance... .... Review and update GMP related SOPs and policies Serve as QA representative on departmental and project team(s) representing CMC...SuggestedFull timeContract workWork at officeLocal area$160.2k - $202.7k
...Associate Director, Quality Assurance, GMP Boston, MA, USA Job Description Posted Friday, December 19, 2025 at 11:00 AM Who... ...Assurance experience, or comparable background of relevant QA experience in drug development in the bio-tech or pharmaceutical...SuggestedFull timeTemporary workWork at officeLocal area2 days per week- ...The Director, Global Product Quality, GMP Processes is a strategic leadership role responsible for benchmarking, standardizing, and optimizing global quality processes across the organization. This role ensures that product quality systems are aligned with Good Manufacturing...SuggestedFull timeWork at office
- ...leading consulting firm in San Francisco is seeking an experienced QA professional specializing in the biotech sector. Candidates... ...have over 10 years of relevant experience and strong expertise in GMP and GCP regulations. The role involves collaboration with CMC teams...SuggestedFull time
- ...Desired Consultant Experience Experienced QA professional or SME within the biotech/biologics sector; monoclonal antibody (mAb) experience... ..., and CRO management Strong working knowledge of applicable GMP and GCP regulations and guidelines (FDA, EMA, ICH) Exceptional...SuggestedFull time
$169k - $200k
...and more efficiently. About the Position The Sr. Manager, GMP Quality Assurance is responsible for ensuring that all GMP-regulated... ...batch records, specifications, protocols, and reports Perform QA review of executed batch records, supporting manufacturing...SuggestedRelocation$160.2k - $202.7k
...with 8+ years of experience in quality assurance within the biotech or pharmaceutical industry. This role requires strong knowledge of GMP regulations and involves managing quality systems, preparing for regulatory inspections, and leading training initiatives. The...SuggestedFull time- ...regulatory compliance, contributing significantly to quality management and product safety. Candidates should have substantial experience in GMP environments and the ability to communicate effectively with regulatory authorities. This role offers the opportunity to impact...Suggested
- ...Quality Assurance Supervisor, you will oversee the Quality Assurance (QA) team and programs for the Womelsdorf, PA site, a manufacturer of... ...Recalls, Food Safety Plans, and pest control systems. Conduct GMP and sanitation audits and summarize technical data to identify...SuggestedFull timeWork at officeImmediate startShift workDay shift
- ...pharmaceuticals, or biotechnology. Demonstrate knowledge of TGA, FDA, and EU GMP and other quality related systems (e.g., ISO Standards, ICH, PIC/s) Job Purpose: ~ Accountable for providing QA Ops management of contractors to ensure compliance with quality and cGMP/...SuggestedFor contractors
$118.4k - $177.6k
Quality Manager The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. This position performs and leads activities "on the floor" in support of batch records review and disposition while ensuring compliance...SuggestedSummer work- ...Assurance Supervisor is responsible for leading, coordinating, and overseeing Quality Assurance (QA) activities to ensure the Company’s Quality Systems comply with applicable GMP, FDA, and internal requirements. This role provides direct supervision to Quality Assurance...SuggestedWork at office
$56.5k - $62.4k
...Assurance team and will perform and administer Quality Assurance (QA) activities at BioLegend, in accordance with BioLegend Vision,... ...minimum of 0-1 work experience in quality assurance. Experience with GMP/GLP or similar regulated products. Experience in MS Word,...SuggestedFull timeWork experience placementWork at officeLocal area- ...is responsible for leading quality systems and ensuring compliance with FDA regulations and GMP standards within a pharmaceutical manufacturing environment. This role oversees QA operations, manages a team, and partners closely with manufacturing, validation, and...Suggested
$22 - $23 per hour
...reports. Train staff on procedures and assist in developing QC/QA methods. Prepare raw material and finished product samples for... ...control Nutraceutical, food & beverage, biotech, pharma (GMP regulated industry working with raw products). Experience with...SuggestedShift workNight shift- ..., and reach those in need. Position Summary The Manager, Quality Assurance will be accountable for all QA activities and decisions to directly support GMP production operations in a Process Execution Team (PET). These activities and decisions include change control...
$28 per hour
...Job Description Salary: $28/Hour Role Summary Reporting to the QA Supervisor, the QA Associate will work within an established culture of Quality Assurance and continuous improvement in all GMP areas. The QA Associate will be directly involved in all areas of...Contract workWork experience placementWork at officeLocal areaMonday to FridayShift workAfternoon shift- ...responsible for managing the day-to-day operations of the 2nd Shift GMP testing group and initiatives. Supervise the team to assure... ...liliFollow required cGMP regulations and assure compliance per internal QA procedures/liliSupervise and approve laboratory quality...Work at officeRelocationMonday to FridayShift workDay shiftAfternoon shift
$41 - $46 per hour
...Required: ~ Bachelor degree in Science Discipline. ~3-5 years of GMP experience, preferably in biologics, audit experience beneficial.... ...Monitor and track actions to closure Job Description: QA Specialist- Audit Readiness (or Senior QA Associate) ~ Supports...- ...Duration : 12 Months Description: Shop Floor QA Specialist QA Shop Floor - 3rd shift Must be able to work four 10 hour days... ...compliance in all my actions by: All employees o Attend GMP training on the schedule designated for my role and as appropriate...Local areaNight shift
$107.1k - $119.92k
...both first and second shifts Supervise one direct report in the QA Tech position Partner with the Planning, Production,... ...legislation on good hygiene practices, good manufacturing practices (GMP's), HACCP, NFPA, OSHA and EPA Ensure compliance and record keeping...Full timeTemporary workLocal areaFlexible hoursShift workWeekend work- ...improvement expectations. The supervisor directs and supports the QA team, verifies critical process controls, ensures consistent and... ...pre-op inspections. Conduct regular line and internal audits, GMP walkthroughs, and documentation reviews to ensure accuracy and compliance...Work at officeShift workNight shiftAfternoon shift
$30 - $40 per hour
...Assurance Specialist I Job Description The Quality Assurance (QA) Specialist I is responsible for ensuring that all products... ...Essential Skills ~ Strong reading comprehension. ~2+ years of GMP experience required. ~ Understanding of batch records and key elements...Contract workTemporary workMonday to Friday- ...procedures while meeting company goals and client requirements. The QA Operations staff reviews all data prior to release and is... ...with laboratory operations, and other departments responsible for GMP activities to resolve deviations and other compliance issues in a...
- ...Job Description Job Description QA Specialist PharmEng Technology has been providing quality services to leading manufacturers... ...development, revision, and implementation of SOPs, protocols, and other GMP documents. Help deliver Deviation, CAPA, and Change Control...Work experience placementLocal area
- ...assigned. Member of CMC Development Teams providing Quality (QA) input from pre-clinical to end of product life cycle including NDA... ...(e.g., final Quality reviewer/approver of Quality events and/or GMP documentation, actively contributes to ongoing investigations as...Full timeLive inRemote workShift work
- ...Reporting to the Site Director, the Senior Quality Manager (QA/QC) is accountable for the overall performance of the site ’s quality... ...standards Oversee all QA/QC activities, ensuring compliance with GMP, HACCP, FSMA, GFSI, and internal quality systems Supervise and...Full timeTemporary workWork at office
- ...product quality. Key Responsibilities: Supervise daily QA/QC activities including receiving, in-process checks, product... ...regulations (AAFCO, FDA, FSMA) Strong understanding of HACCP, GMP, and GFSI standards Excellent communication, leadership, and problem...Full timeWork at officeShift work
$63k - $93k
...standards. You will play a key role in audits, HACCP program evaluation, GMP training, sanitation assessments, pest control, and resolving... ...supplies • Provide technical assistance and training to QA personnel • Monitor and verify HACCP plan CCPs, ensuring adherence...Local areaFlexible hoursNight shift$243.1k - $314.6k
...approaches and periodic management reviews. Run an independent QA function with authority for final batch disposition and QA... ...responsibilities: complaints handling, investigations, escalation of serious GMP issues, internal audits/selfinspection, and training...Full timeLocal area









